Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
T |
C |
5: 109,736,324 (GRCm38) |
|
probably null |
Het |
Abcc12 |
C |
T |
8: 86,553,391 (GRCm38) |
E338K |
probably benign |
Het |
Abcc5 |
A |
T |
16: 20,372,156 (GRCm38) |
S815T |
probably benign |
Het |
Ankrd16 |
G |
A |
2: 11,789,808 (GRCm38) |
E335K |
probably benign |
Het |
Atm |
A |
G |
9: 53,503,075 (GRCm38) |
F905S |
possibly damaging |
Het |
Bckdha |
C |
T |
7: 25,631,652 (GRCm38) |
R281H |
probably damaging |
Het |
Blvra |
C |
T |
2: 127,095,191 (GRCm38) |
T188I |
probably damaging |
Het |
Bmp8b |
C |
A |
4: 123,116,168 (GRCm38) |
|
probably benign |
Het |
Cacna2d3 |
A |
G |
14: 29,347,120 (GRCm38) |
|
probably null |
Het |
Cacng8 |
T |
C |
7: 3,394,474 (GRCm38) |
S84P |
probably damaging |
Het |
Cad |
T |
A |
5: 31,061,650 (GRCm38) |
V605E |
probably damaging |
Het |
Ccny |
A |
G |
18: 9,449,641 (GRCm38) |
S11P |
probably benign |
Het |
Col3a1 |
C |
A |
1: 45,321,990 (GRCm38) |
P112T |
unknown |
Het |
Corin |
T |
C |
5: 72,422,165 (GRCm38) |
E155G |
probably benign |
Het |
Cyp27a1 |
A |
G |
1: 74,737,559 (GRCm38) |
E501G |
probably damaging |
Het |
Dennd3 |
T |
A |
15: 73,542,732 (GRCm38) |
N457K |
possibly damaging |
Het |
Dnah7a |
T |
G |
1: 53,501,656 (GRCm38) |
I2520L |
probably benign |
Het |
Dst |
C |
T |
1: 34,212,319 (GRCm38) |
S4165F |
probably damaging |
Het |
Fgf14 |
A |
C |
14: 123,980,389 (GRCm38) |
I234R |
probably benign |
Het |
Foxp4 |
A |
G |
17: 47,875,528 (GRCm38) |
I442T |
unknown |
Het |
Gad2 |
T |
G |
2: 22,684,988 (GRCm38) |
D472E |
probably benign |
Het |
Garnl3 |
G |
T |
2: 32,992,228 (GRCm38) |
H832N |
probably benign |
Het |
Gm13941 |
T |
C |
2: 111,104,853 (GRCm38) |
M11V |
unknown |
Het |
Gnptab |
T |
A |
10: 88,433,577 (GRCm38) |
L714* |
probably null |
Het |
Golgb1 |
C |
A |
16: 36,898,733 (GRCm38) |
Q334K |
probably benign |
Het |
Gp9 |
A |
G |
6: 87,779,151 (GRCm38) |
I49M |
probably benign |
Het |
Guf1 |
A |
G |
5: 69,561,157 (GRCm38) |
N213S |
probably damaging |
Het |
H2-K1 |
T |
G |
17: 33,997,329 (GRCm38) |
H281P |
probably damaging |
Het |
Hhip |
T |
A |
8: 79,997,495 (GRCm38) |
M373L |
probably benign |
Het |
Ifi203 |
C |
T |
1: 173,933,796 (GRCm38) |
C229Y |
possibly damaging |
Het |
Ighv13-2 |
A |
G |
12: 114,357,798 (GRCm38) |
L88S |
probably damaging |
Het |
Kcna3 |
T |
C |
3: 107,036,696 (GRCm38) |
Y92H |
possibly damaging |
Het |
Lmo7 |
A |
G |
14: 101,922,095 (GRCm38) |
|
probably null |
Het |
Lrguk |
A |
G |
6: 34,073,768 (GRCm38) |
D387G |
probably damaging |
Het |
Mki67 |
A |
C |
7: 135,696,130 (GRCm38) |
S2392A |
probably benign |
Het |
Mknk2 |
C |
T |
10: 80,667,975 (GRCm38) |
W367* |
probably null |
Het |
Mocos |
A |
G |
18: 24,676,662 (GRCm38) |
K441E |
probably damaging |
Het |
Mpnd |
T |
C |
17: 56,011,692 (GRCm38) |
S150P |
probably damaging |
Het |
Naip2 |
A |
T |
13: 100,179,432 (GRCm38) |
L280Q |
probably damaging |
Het |
Naip2 |
G |
C |
13: 100,179,433 (GRCm38) |
L280V |
probably damaging |
Het |
Neurod4 |
C |
T |
10: 130,270,482 (GRCm38) |
V308I |
probably benign |
Het |
Nxf3 |
C |
T |
X: 136,073,983 (GRCm38) |
V474I |
probably benign |
Het |
Or10d5j |
A |
T |
9: 39,956,581 (GRCm38) |
M118K |
probably damaging |
Het |
Or8u10 |
A |
T |
2: 86,085,407 (GRCm38) |
Y123* |
probably null |
Het |
Pam |
T |
A |
1: 97,854,756 (GRCm38) |
|
probably benign |
Het |
Pde5a |
T |
C |
3: 122,803,160 (GRCm38) |
Y467H |
probably damaging |
Het |
Pibf1 |
T |
A |
14: 99,137,121 (GRCm38) |
V332E |
possibly damaging |
Het |
Plxna1 |
C |
A |
6: 89,356,519 (GRCm38) |
R376L |
probably damaging |
Het |
Proz |
A |
G |
8: 13,073,533 (GRCm38) |
E268G |
probably benign |
Het |
Rimbp3 |
A |
T |
16: 17,210,299 (GRCm38) |
H529L |
probably benign |
Het |
Rnf103 |
C |
G |
6: 71,508,875 (GRCm38) |
C163W |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,512,296 (GRCm38) |
V1433A |
probably damaging |
Het |
Septin11 |
G |
T |
5: 93,162,167 (GRCm38) |
M276I |
probably damaging |
Het |
Slc30a4 |
A |
G |
2: 122,702,272 (GRCm38) |
V50A |
probably damaging |
Het |
Sorbs1 |
A |
G |
19: 40,314,443 (GRCm38) |
V570A |
probably damaging |
Het |
Spout1 |
T |
C |
2: 30,177,407 (GRCm38) |
|
probably null |
Het |
Syne2 |
T |
C |
12: 76,048,622 (GRCm38) |
L5241P |
probably damaging |
Het |
Tas2r110 |
T |
A |
6: 132,868,675 (GRCm38) |
I223N |
probably damaging |
Het |
Tead2 |
T |
A |
7: 45,232,328 (GRCm38) |
|
probably null |
Het |
Thsd1 |
A |
G |
8: 22,259,411 (GRCm38) |
H713R |
probably damaging |
Het |
Ttc21b |
A |
G |
2: 66,242,679 (GRCm38) |
L221S |
probably damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm38) |
P46S |
probably benign |
Het |
Vmn2r105 |
A |
G |
17: 20,208,690 (GRCm38) |
I708T |
possibly damaging |
Het |
Vmn2r117 |
G |
T |
17: 23,460,415 (GRCm38) |
H612N |
probably damaging |
Het |
Wnk1 |
C |
T |
6: 119,969,354 (GRCm38) |
G613S |
possibly damaging |
Het |
Zbtb41 |
T |
A |
1: 139,423,996 (GRCm38) |
H282Q |
probably benign |
Het |
Zfp335 |
C |
A |
2: 164,900,106 (GRCm38) |
|
probably null |
Het |
Zmym2 |
T |
A |
14: 56,921,499 (GRCm38) |
|
probably benign |
Het |
|
Other mutations in Cul9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Cul9
|
APN |
17 |
46,525,709 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00330:Cul9
|
APN |
17 |
46,510,841 (GRCm38) |
splice site |
probably benign |
|
IGL00726:Cul9
|
APN |
17 |
46,528,096 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01020:Cul9
|
APN |
17 |
46,539,023 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01358:Cul9
|
APN |
17 |
46,538,314 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01410:Cul9
|
APN |
17 |
46,528,646 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01781:Cul9
|
APN |
17 |
46,539,304 (GRCm38) |
missense |
probably benign |
|
IGL01873:Cul9
|
APN |
17 |
46,502,452 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02117:Cul9
|
APN |
17 |
46,540,375 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02300:Cul9
|
APN |
17 |
46,521,032 (GRCm38) |
splice site |
probably benign |
|
IGL02426:Cul9
|
APN |
17 |
46,523,258 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL02427:Cul9
|
APN |
17 |
46,502,632 (GRCm38) |
missense |
possibly damaging |
0.69 |
IGL02496:Cul9
|
APN |
17 |
46,540,376 (GRCm38) |
missense |
possibly damaging |
0.72 |
IGL03008:Cul9
|
APN |
17 |
46,502,697 (GRCm38) |
splice site |
probably benign |
|
IGL03059:Cul9
|
APN |
17 |
46,538,987 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL03302:Cul9
|
APN |
17 |
46,526,640 (GRCm38) |
missense |
probably damaging |
0.98 |
bottlenose
|
UTSW |
17 |
46,500,844 (GRCm38) |
missense |
possibly damaging |
0.79 |
flipper
|
UTSW |
17 |
46,525,892 (GRCm38) |
missense |
probably benign |
0.05 |
orca
|
UTSW |
17 |
46,525,135 (GRCm38) |
missense |
probably damaging |
1.00 |
FR4340:Cul9
|
UTSW |
17 |
46,500,853 (GRCm38) |
small insertion |
probably benign |
|
FR4449:Cul9
|
UTSW |
17 |
46,500,856 (GRCm38) |
small insertion |
probably benign |
|
FR4737:Cul9
|
UTSW |
17 |
46,500,858 (GRCm38) |
small insertion |
probably benign |
|
FR4737:Cul9
|
UTSW |
17 |
46,500,846 (GRCm38) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,500,853 (GRCm38) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,500,850 (GRCm38) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,500,848 (GRCm38) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,500,856 (GRCm38) |
small insertion |
probably benign |
|
R0012:Cul9
|
UTSW |
17 |
46,538,510 (GRCm38) |
missense |
probably benign |
0.26 |
R0079:Cul9
|
UTSW |
17 |
46,537,663 (GRCm38) |
nonsense |
probably null |
|
R0143:Cul9
|
UTSW |
17 |
46,526,410 (GRCm38) |
missense |
possibly damaging |
0.65 |
R0390:Cul9
|
UTSW |
17 |
46,528,589 (GRCm38) |
missense |
probably benign |
0.34 |
R0401:Cul9
|
UTSW |
17 |
46,541,704 (GRCm38) |
missense |
probably damaging |
1.00 |
R0529:Cul9
|
UTSW |
17 |
46,520,468 (GRCm38) |
splice site |
probably benign |
|
R0815:Cul9
|
UTSW |
17 |
46,537,822 (GRCm38) |
splice site |
probably null |
|
R0863:Cul9
|
UTSW |
17 |
46,537,822 (GRCm38) |
splice site |
probably null |
|
R0972:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1173:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1216:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1217:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1261:Cul9
|
UTSW |
17 |
46,525,782 (GRCm38) |
missense |
probably damaging |
1.00 |
R1278:Cul9
|
UTSW |
17 |
46,500,849 (GRCm38) |
small deletion |
probably benign |
|
R1281:Cul9
|
UTSW |
17 |
46,511,534 (GRCm38) |
missense |
probably damaging |
1.00 |
R1349:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1372:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1403:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1403:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1405:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1405:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R1467:Cul9
|
UTSW |
17 |
46,525,373 (GRCm38) |
missense |
probably damaging |
1.00 |
R1467:Cul9
|
UTSW |
17 |
46,525,373 (GRCm38) |
missense |
probably damaging |
1.00 |
R1482:Cul9
|
UTSW |
17 |
46,508,547 (GRCm38) |
missense |
probably damaging |
0.99 |
R1491:Cul9
|
UTSW |
17 |
46,538,564 (GRCm38) |
nonsense |
probably null |
|
R1618:Cul9
|
UTSW |
17 |
46,525,892 (GRCm38) |
missense |
probably benign |
0.05 |
R1641:Cul9
|
UTSW |
17 |
46,543,560 (GRCm38) |
missense |
possibly damaging |
0.96 |
R1679:Cul9
|
UTSW |
17 |
46,521,156 (GRCm38) |
missense |
possibly damaging |
0.90 |
R1771:Cul9
|
UTSW |
17 |
46,537,812 (GRCm38) |
missense |
probably benign |
0.41 |
R1803:Cul9
|
UTSW |
17 |
46,503,097 (GRCm38) |
missense |
probably damaging |
1.00 |
R2020:Cul9
|
UTSW |
17 |
46,522,175 (GRCm38) |
missense |
probably damaging |
1.00 |
R2046:Cul9
|
UTSW |
17 |
46,543,733 (GRCm38) |
missense |
probably damaging |
1.00 |
R2056:Cul9
|
UTSW |
17 |
46,543,372 (GRCm38) |
missense |
probably benign |
|
R2088:Cul9
|
UTSW |
17 |
46,526,649 (GRCm38) |
missense |
probably damaging |
1.00 |
R2415:Cul9
|
UTSW |
17 |
46,543,438 (GRCm38) |
missense |
probably benign |
|
R2925:Cul9
|
UTSW |
17 |
46,510,981 (GRCm38) |
missense |
probably benign |
0.08 |
R2964:Cul9
|
UTSW |
17 |
46,502,228 (GRCm38) |
missense |
probably damaging |
0.96 |
R2965:Cul9
|
UTSW |
17 |
46,502,228 (GRCm38) |
missense |
probably damaging |
0.96 |
R3690:Cul9
|
UTSW |
17 |
46,504,031 (GRCm38) |
splice site |
probably null |
|
R4437:Cul9
|
UTSW |
17 |
46,502,159 (GRCm38) |
missense |
probably damaging |
1.00 |
R4470:Cul9
|
UTSW |
17 |
46,538,336 (GRCm38) |
missense |
probably benign |
0.00 |
R4540:Cul9
|
UTSW |
17 |
46,503,089 (GRCm38) |
missense |
probably null |
0.98 |
R4555:Cul9
|
UTSW |
17 |
46,501,829 (GRCm38) |
missense |
possibly damaging |
0.82 |
R4604:Cul9
|
UTSW |
17 |
46,530,146 (GRCm38) |
missense |
probably damaging |
0.99 |
R4646:Cul9
|
UTSW |
17 |
46,539,017 (GRCm38) |
nonsense |
probably null |
|
R4799:Cul9
|
UTSW |
17 |
46,500,844 (GRCm38) |
missense |
possibly damaging |
0.79 |
R4822:Cul9
|
UTSW |
17 |
46,530,051 (GRCm38) |
missense |
probably benign |
0.01 |
R4964:Cul9
|
UTSW |
17 |
46,538,525 (GRCm38) |
missense |
probably damaging |
1.00 |
R4965:Cul9
|
UTSW |
17 |
46,538,525 (GRCm38) |
missense |
probably damaging |
1.00 |
R5027:Cul9
|
UTSW |
17 |
46,500,782 (GRCm38) |
missense |
probably damaging |
0.99 |
R5185:Cul9
|
UTSW |
17 |
46,525,832 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5237:Cul9
|
UTSW |
17 |
46,543,467 (GRCm38) |
missense |
probably benign |
0.00 |
R5278:Cul9
|
UTSW |
17 |
46,510,873 (GRCm38) |
missense |
probably damaging |
1.00 |
R5361:Cul9
|
UTSW |
17 |
46,500,849 (GRCm38) |
small deletion |
probably benign |
|
R5455:Cul9
|
UTSW |
17 |
46,510,846 (GRCm38) |
splice site |
probably null |
|
R5592:Cul9
|
UTSW |
17 |
46,520,591 (GRCm38) |
missense |
probably benign |
0.00 |
R5597:Cul9
|
UTSW |
17 |
46,502,665 (GRCm38) |
missense |
possibly damaging |
0.56 |
R5613:Cul9
|
UTSW |
17 |
46,503,844 (GRCm38) |
missense |
probably damaging |
1.00 |
R6122:Cul9
|
UTSW |
17 |
46,521,928 (GRCm38) |
missense |
possibly damaging |
0.72 |
R6135:Cul9
|
UTSW |
17 |
46,521,453 (GRCm38) |
missense |
probably benign |
|
R6352:Cul9
|
UTSW |
17 |
46,511,315 (GRCm38) |
missense |
probably benign |
0.00 |
R6376:Cul9
|
UTSW |
17 |
46,508,563 (GRCm38) |
missense |
probably damaging |
1.00 |
R6868:Cul9
|
UTSW |
17 |
46,522,183 (GRCm38) |
missense |
possibly damaging |
0.73 |
R6898:Cul9
|
UTSW |
17 |
46,511,026 (GRCm38) |
missense |
possibly damaging |
0.87 |
R7090:Cul9
|
UTSW |
17 |
46,500,839 (GRCm38) |
missense |
probably damaging |
0.96 |
R7193:Cul9
|
UTSW |
17 |
46,538,497 (GRCm38) |
missense |
probably damaging |
0.98 |
R7221:Cul9
|
UTSW |
17 |
46,528,565 (GRCm38) |
missense |
probably damaging |
0.99 |
R7291:Cul9
|
UTSW |
17 |
46,540,433 (GRCm38) |
missense |
probably benign |
0.00 |
R7320:Cul9
|
UTSW |
17 |
46,510,909 (GRCm38) |
missense |
possibly damaging |
0.80 |
R7348:Cul9
|
UTSW |
17 |
46,510,993 (GRCm38) |
missense |
possibly damaging |
0.89 |
R7463:Cul9
|
UTSW |
17 |
46,520,476 (GRCm38) |
splice site |
probably null |
|
R7480:Cul9
|
UTSW |
17 |
46,537,812 (GRCm38) |
missense |
probably benign |
0.41 |
R7573:Cul9
|
UTSW |
17 |
46,519,910 (GRCm38) |
missense |
probably benign |
|
R7582:Cul9
|
UTSW |
17 |
46,510,979 (GRCm38) |
missense |
probably damaging |
1.00 |
R7605:Cul9
|
UTSW |
17 |
46,541,732 (GRCm38) |
missense |
probably damaging |
0.99 |
R7684:Cul9
|
UTSW |
17 |
46,509,889 (GRCm38) |
missense |
probably damaging |
1.00 |
R7830:Cul9
|
UTSW |
17 |
46,540,311 (GRCm38) |
missense |
probably benign |
0.37 |
R7834:Cul9
|
UTSW |
17 |
46,525,704 (GRCm38) |
splice site |
probably null |
|
R8131:Cul9
|
UTSW |
17 |
46,511,242 (GRCm38) |
missense |
probably damaging |
1.00 |
R8192:Cul9
|
UTSW |
17 |
46,538,347 (GRCm38) |
missense |
probably benign |
0.01 |
R8231:Cul9
|
UTSW |
17 |
46,520,501 (GRCm38) |
missense |
probably damaging |
0.99 |
R8248:Cul9
|
UTSW |
17 |
46,530,014 (GRCm38) |
missense |
probably damaging |
0.99 |
R8504:Cul9
|
UTSW |
17 |
46,503,580 (GRCm38) |
missense |
probably damaging |
1.00 |
R8550:Cul9
|
UTSW |
17 |
46,519,846 (GRCm38) |
missense |
probably damaging |
1.00 |
R8716:Cul9
|
UTSW |
17 |
46,527,914 (GRCm38) |
missense |
probably benign |
0.28 |
R8769:Cul9
|
UTSW |
17 |
46,521,902 (GRCm38) |
missense |
possibly damaging |
0.85 |
R8893:Cul9
|
UTSW |
17 |
46,500,849 (GRCm38) |
small deletion |
probably benign |
|
R8904:Cul9
|
UTSW |
17 |
46,520,501 (GRCm38) |
missense |
probably damaging |
0.99 |
R8936:Cul9
|
UTSW |
17 |
46,528,602 (GRCm38) |
missense |
possibly damaging |
0.82 |
R8972:Cul9
|
UTSW |
17 |
46,543,251 (GRCm38) |
missense |
probably damaging |
1.00 |
R9003:Cul9
|
UTSW |
17 |
46,525,075 (GRCm38) |
missense |
possibly damaging |
0.78 |
R9012:Cul9
|
UTSW |
17 |
46,543,521 (GRCm38) |
missense |
probably benign |
|
R9056:Cul9
|
UTSW |
17 |
46,543,770 (GRCm38) |
missense |
probably damaging |
0.99 |
R9071:Cul9
|
UTSW |
17 |
46,526,453 (GRCm38) |
missense |
probably benign |
|
R9162:Cul9
|
UTSW |
17 |
46,526,603 (GRCm38) |
missense |
probably benign |
0.32 |
R9476:Cul9
|
UTSW |
17 |
46,510,907 (GRCm38) |
missense |
probably damaging |
1.00 |
R9526:Cul9
|
UTSW |
17 |
46,530,100 (GRCm38) |
missense |
probably benign |
0.41 |
R9563:Cul9
|
UTSW |
17 |
46,509,971 (GRCm38) |
missense |
probably benign |
0.01 |
R9568:Cul9
|
UTSW |
17 |
46,520,118 (GRCm38) |
missense |
possibly damaging |
0.56 |
R9610:Cul9
|
UTSW |
17 |
46,519,897 (GRCm38) |
missense |
possibly damaging |
0.96 |
R9611:Cul9
|
UTSW |
17 |
46,519,897 (GRCm38) |
missense |
possibly damaging |
0.96 |
R9705:Cul9
|
UTSW |
17 |
46,543,300 (GRCm38) |
missense |
probably damaging |
1.00 |
R9765:Cul9
|
UTSW |
17 |
46,539,298 (GRCm38) |
missense |
probably benign |
0.18 |
RF011:Cul9
|
UTSW |
17 |
46,500,848 (GRCm38) |
small insertion |
probably benign |
|
RF016:Cul9
|
UTSW |
17 |
46,500,863 (GRCm38) |
nonsense |
probably null |
|
RF026:Cul9
|
UTSW |
17 |
46,500,869 (GRCm38) |
nonsense |
probably null |
|
RF027:Cul9
|
UTSW |
17 |
46,500,848 (GRCm38) |
small insertion |
probably benign |
|
RF030:Cul9
|
UTSW |
17 |
46,500,869 (GRCm38) |
small insertion |
probably benign |
|
RF033:Cul9
|
UTSW |
17 |
46,500,854 (GRCm38) |
small insertion |
probably benign |
|
RF039:Cul9
|
UTSW |
17 |
46,500,854 (GRCm38) |
small insertion |
probably benign |
|
RF041:Cul9
|
UTSW |
17 |
46,500,854 (GRCm38) |
nonsense |
probably null |
|
RF042:Cul9
|
UTSW |
17 |
46,540,615 (GRCm38) |
frame shift |
probably null |
|
RF057:Cul9
|
UTSW |
17 |
46,500,863 (GRCm38) |
nonsense |
probably null |
|
Z1176:Cul9
|
UTSW |
17 |
46,520,585 (GRCm38) |
nonsense |
probably null |
|
Z1176:Cul9
|
UTSW |
17 |
46,520,576 (GRCm38) |
nonsense |
probably null |
|
Z1177:Cul9
|
UTSW |
17 |
46,537,797 (GRCm38) |
missense |
probably benign |
0.14 |
|